CVS stops sale of heartburn drugs with suspect contaminant
CVS has halted sales of popular heartburn treatment Zantac and its generic store brand after warnings by U.S. health regulators.
It’s the latest precautionary move by retailers and manufacturers after the U.S. Food and Drug Administration recently warned consumers about a potentially dangerous contaminant in prescription and over-the-counter versions of Zantac.
In its announcement this weekend, CVS said customers who bought Zantac products can return them for a refund. The retailer will continue to sell other heartburn medications.
WHAT’S THE ISSUE?
In September, the FDA said it detected low levels of a probable cancer-causing chemical known as NDMA in Zantac and related generic drugs to treat ulcers and reflux disease. The same chemical has been linked to dozens of recalls of prescription blood pressure drugs in the past year.
The agency said the amount found in Zantac products barely exceeds levels found in common foods such as meats, dairy products and chemicals. Even so, the warning has led some pharmacies and manufacturers to stop selling drugs containing Zantac’s active ingredient, ranitidine.
WHAT’S THE REACTION?
CVS Health said Saturday it has pulled Zantac and its generic store brand, saying the move “is being taken out of an abundance of caution.” On Monday, Rite Aid said it’s removing Zantac and related drugs sold under its name from its shelves. Walgreens earlier said it’s removing Zantac products from shelves while the FDA continues its investigation.
Last week, two generic makers voluntarily recalled their products: Apotex and Sandoz, the generic unit of drug giant Novartis AG. Both companies said they haven’t received any reports of patient harm. Some other manufacturers have stopped shipping their product to pharmacies.
The recalled Apotex products are sold at and labeled by Walgreens, Walmart and Rite-Aid, according to the FDA.
Sanofi, which makes brand name Zantac, said Monday it’s working with the FDA and doing its own investigation. But it has not stopped selling Zantac in the U.S.
The FDA has asked makers of ranitidine medications to test levels of NDMA in their products and to send samples to the agency.
WHAT’S THE ADVICE FOR PATIENTS?
Currently, the FDA isn’t advising patients to stop taking Zantac and related drugs. The agency said not all ranitidine medicines sold in the U.S. are being recalled. Concerned patients should contact their doctor.
ARE THERE ALTERNATIVES?
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